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首页> 外文期刊>Journal of land use science >Performance evaluation of Active Melioidosis Detect-Lateral Flow Assay (AMD-LFA) for diagnosis of melioidosis in endemic settings with limited resources
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Performance evaluation of Active Melioidosis Detect-Lateral Flow Assay (AMD-LFA) for diagnosis of melioidosis in endemic settings with limited resources

机译:活性融合检测横向流动测定(AMD-LFA)的性能评价用于诊断资源有限的地方性环境中的融合中

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Melioidosis is a fatal infection caused by the soil saprophyte Burkholderia pseudomallei. Early diagnosis and befitting medical management can significantly influence the clinical outcomes among patients with melioidosis. Witnessing an annual increment in the number of melioidosis cases, over the past few years, mainly from the developing tropical nations, the present study was undertaken to evaluate the diagnostic utility of Active Melioidosis Detect (TM) LateralFlow Assay (AMD-LFA), in comparison with enrichment culture and PCR. A total of 206clinical specimens obtained from 175 patients with clinical suspicion of melioidosis were considered for the evaluation. Positivity for B.pseudomallei using enrichment culture, PCR and AMD-LFA were observed among 63 (30.5%), 55 (26.6%) and 63 (30.5%) specimens respectively. The AMD-LFA failed to detect melioidosis from 9 culture-confirmed cases (6 whole blood specimens, 2 pus samples, and one synovial fluid). Further the test gave faint bands from 9 urine samples which were negative by culture and PCR. AMD-LFA demonstrated a sensitivity, specificity, of 85.71%(CI:74.61% to 93.25%) and 93.62% (Cl:88.23% to 97.04%), with positive predictive value of 85.71% (CI: 75.98% to 91.92%) and negative predictive value of 93.62% (Cl:88.89% to 96.42%). The test needs further evaluation in view of the faint bands from negative urine samples, for incorporating the test as a point of care assay. In view of its rapidity and ease of testing AMD-LFA might be useful in early diagnosis of melioidosis at resource constraint settings.
机译:醚类是由土壤皂细胞Burkholderia Pseudomallei引起的致命感染。早期诊断和健康的医学管理可以显着影响培养患者患者的临床结果。在过去几年中,目睹了春季病例的年增长率,主要来自发展中的热带国家,本研究旨在评估活性融合检测​​(TM)左侧测定(AMD-LFA)的诊断效用与富集培养和PCR的比较。从175例临床暂性患者中获得共有206克隆的标本,考虑了评估。在63(30.5%),55%(26.6%)和63(30.5%)标本中,观察到使用富集培养,PCR和AMD-LFA的B.Pseudomallei的阳性。 AMD-LFA未能检测9种培养确诊病例(6个全血样标本,2个脓样品和一个滑液)的混合症。此外,测试给出了来自9个尿液样品的微弱条带,其是培养物和PCR阴性的。 AMD-LFA证明了敏感性,特异性为85.71%(CI:74.61%至93.25%)和93.62%(CL:88.23%至97.04%),阳性预测值为85.71%(CI:75.98%至91.92%)和负面预测值为93.62%(CL:88.89%至96.42%)。考试需要进一步评价对于来自阴性尿液样本的微弱带,以将测试作为护理点测定。鉴于其快速和易于测力,AMD-LFA可能在资源限制环境下的早期诊断融合中。

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